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Clinical Trials/KCT0004022
KCT0004022
Completed
未知

Skin Primary Irritation Test in Humans

Dermapro0 sites30 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Dermapro
Enrollment
30
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional Study
Sex
Female

Investigators

Sponsor
Dermapro

Eligibility Criteria

Inclusion Criteria

  • ?Healthy females or males aged 20 to 60 years
  • ?Subjects who signed the informed consent; the purpose and the protocol of the study are explained to subjects.
  • ?Subjects who are willing to cooperate with the requirements of the study during the test period and contact investigator immediately if they experience any adverse reaction.
  • ?Subjects should be cooperative and available for follow\-up during the study period.

Exclusion Criteria

  • ?Women who are self\-reported pregnant, nursing or planning a pregnancy
  • ?Subjects with a history of any dermatological disease or condition, including but not limited to active atopic dermatitis, psoriasis, eczema, active seasonal allergies within the past a months
  • ?Subjects with abnormal skin pigmentation at the test sites which might interfere with subsequent evaluations of dermal responsiveness
  • ?Subjects taking medications which might interfere with the test results, including anti\-inflammatory, antihistamines or immunosuppressive drugs
  • ?Subjects who have applied any type of topical anti\-inflammatory medication to the test sites within two weeks prior to enrollment
  • ?Subjects with any other skin condition that would interfere with the conduct of the study
  • ?Subjects with a history of immune deficiency or auto\-immune disease
  • ?Subjects who are currently receiving allergy injections, have received allergy injections within one week prior to enrollment, or expect to begin receiving allergy injections during the study
  • ?Subjects who are currently under treatment for chronic diseases (asthma and diabetes etc.)
  • ?Current enrollment in any other research study or participation in a patch test study within 30 days prior to the start of this study

Outcomes

Primary Outcomes

Not specified

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